H. Archer

Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X chromosome inactivation. (2007)

Clarke, Angus John, Archer, H., Leonard, H., Evans, J.

Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X chromosome inactivation. (2007)

Clarke, Angus John, Archer, H., Leonard, H., Evans, J.

Dimensional phenotypic analysis and functional categorisation of mutations reveal novel genotype–phenotype associations in Rett syndrome (2005)

Charman, T., Neilson, T.C.S., Mash, V., Archer, H., Gardiner, M.T., Knudsen, G.P.S., ...

We aimed to improve the understanding of genotype–phenotype correlations in Rett syndrome (RS) by adopting a novel approach to categorising phenotypic dimensions – separating typicality of...

Early onset seizures and Rett-like features associated with mutations in CDKL5 (2005)

Evans, J., Archer, H., Colley, J. P., Ravn, K., Nielsen, J. B., Kerr, A., ...

Early onset seizures and Rett-like features associated with mutations in CDKL5 (2005)

Evans, J., Archer, H., Colley, J. P., Ravn, K., Nielsen, J. B., Kerr, A., ...

Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation (2004)

Weaving, L. S., Christodoulou, J., Williamson, S. L., Friend, K. L., McKenzie, O. L.D., Archer, H., ...

Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation (2004)

Weaving, L. S., Christodoulou, J., Williamson, S. L., Friend, K. L., McKenzie, O. L.D., Archer, H., ...